Canonical Allele Identifier: CA265710191

Gene: RIN3

Linked Data

• dbSNP Id: rs61992591
• MyVariant Identifiers: chr14:g.93103251A>T (hg19) ; chr14:g.92636906A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92636906A>T , CM000676.2:g.92636906A>T	GRCh38
NC_000014.8:g.93103251A>T , CM000676.1:g.93103251A>T	GRCh37
NC_000014.7:g.92173004A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216487.12:c.441-4332A>T MANE Select	ENSP00000216487.7:n.441-4332A>T
ENST00000216487.11:c.441-4332A>T	ENSP00000216487.7:n.441-4332A>T
ENST00000418924.6:n.340-4332A>T
ENST00000554888.1:n.8-4332A>T
ENST00000555589.5:c.368-4332A>T	ENSP00000450682.1:n.368-4332A>T
ENST00000620541.4:c.441-4332A>T	ENSP00000480603.1:n.441-4332A>T
NM_024832.3:c.441-4332A>T	NP_079108.3:n.441-4332A>T
XM_011537163.1:c.216-4332A>T	XP_011535465.1:n.216-4332A>T
XM_011537164.1:c.213-4332A>T	XP_011535466.1:n.213-4332A>T
XM_011537165.1:c.-571-4332A>T	XP_011535467.1:n.-571-4332A>T
NM_001319987.1:c.216-4332A>T	NP_001306916.1:n.216-4332A>T
NM_024832.4:c.441-4332A>T	NP_079108.3:n.441-4332A>T
XM_011537164.3:c.213-4332A>T	XP_011535466.1:n.213-4332A>T
XM_011537165.3:c.-571-4332A>T	XP_011535467.1:n.-571-4332A>T
XM_017021651.2:c.348-4332A>T	XP_016877140.1:n.348-4332A>T
XM_017021652.1:c.441-4332A>T	XP_016877141.1:n.441-4332A>T
XM_017021653.1:c.441-4332A>T	XP_016877142.1:n.441-4332A>T
XM_017021654.1:c.441-4332A>T	XP_016877143.1:n.441-4332A>T
NM_024832.5:c.441-4332A>T MANE Select	NP_079108.3:n.441-4332A>T
NM_001319987.2:c.216-4332A>T	NP_001306916.1:n.216-4332A>T